Delayed Diagnosis of SMARCA4-Deficient Undifferentiated Tumor in a Heavy Smoker Male Patient: Discovered Through Bone Sampling, with Extensive Distant Metastases and Concurrent Granulomatous Disease, Leading to Patient Fatality.

IF 0.9 4区 医学 Q4 PATHOLOGY
Nada Shaker, Ruwaida Ben Musa, Zofia Tynski, Nuha Shaker, Omar P Sangueza, Brandon Boyd
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Abstract

Background. SMARCA4-deficient undifferentiated tumors are rare and pose a diagnostic challenge. This study delves into the intricate diagnostic terrain of SMARCA4-deficient undifferentiated tumors, providing insights into their diverse clinical presentations and diagnostic approaches. Case Presentation. A 69-year-old heavy-smoker man with adalimumab-treated rheumatoid arthritis presented with multiple lesions. A CT scan revealed a spiculated lung mass, enlarged mediastinal lymph nodes, and hepatic lesions. A whole-body FDG-PET/CT scan revealed heterogeneous hypermetabolic lesions in the lung, liver, and bone. Initial two core needle liver biopsies and a left upper lobe lung wedge resection initially indicated steatohepatitis and granulomatous formation with no evidence of malignancy. Several months later, the patient returned with left-sided flank pain and significant weight loss. CT scan identified a thigh mass, adrenal lesion, and extensive multiple skeletal lesions. A biopsy of the thigh mass revealed an extensively necrotic, epithelioid-to-spindled cell neoplasm with positive staining for pan keratin, focal staining for CD56, and a loss of nuclear expression of SMARCA4. A final diagnosis of SMARCA4-deficient undifferentiated tumor was rendered. Unfortunately, the patient's condition deteriorated, and he died a few weeks after receiving the final diagnosis. Conclusion. SMARCA4-deficient undifferentiated tumors have emerged as recent subjects of medical study, distinguished by their unique morphology and SMARCA4-deficient immunohistochemistry. These tumors present diverse clinical manifestations, affecting multiple organ systems. This report underscores the diagnostic complexities associated with complex clinical presentation and highlights the importance of multidisciplinary collaboration in addressing challenging clinical scenarios, particularly among heavy smoker male patients and intricate radiological presentations.

重度吸烟男性患者的 SMARCA4 缺失性未分化肿瘤诊断延迟:通过骨取样发现的广泛远处转移瘤和并发肉芽肿病导致患者死亡。
背景。SMARCA4缺陷型未分化肿瘤非常罕见,是诊断上的一个难题。本研究深入探讨了SMARCA4缺陷型未分化肿瘤错综复杂的诊断过程,对其不同的临床表现和诊断方法提出了见解。病例介绍。一名 69 岁的重度吸烟男子,患有阿达木单抗治疗的类风湿性关节炎,并伴有多处病变。CT 扫描显示肺部肿块、纵隔淋巴结肿大和肝脏病变。全身 FDG-PET/CT 扫描显示肺部、肝脏和骨骼存在异质性高代谢病变。最初的两次核心肝穿刺活检和一次左上肺叶楔形切除术显示,患者患有脂肪性肝炎和肉芽肿形成,但无恶性证据。几个月后,患者因左侧腹痛和体重明显减轻复诊。CT 扫描发现大腿肿块、肾上腺病变和广泛的多发性骨骼病变。大腿肿块活检显示为广泛坏死的上皮样至棘细胞肿瘤,泛角蛋白染色阳性,CD56局灶性染色,SMARCA4核表达缺失。最终诊断为 SMARCA4 缺乏性未分化肿瘤。不幸的是,患者病情恶化,在得到最终诊断几周后死亡。结论SMARCA4缺陷型未分化肿瘤以其独特的形态和SMARCA4缺陷型免疫组化而成为近年来医学研究的热点。这些肿瘤的临床表现多种多样,影响多个器官系统。本报告强调了与复杂临床表现相关的诊断复杂性,并强调了多学科合作在应对具有挑战性的临床情况中的重要性,尤其是在重度吸烟的男性患者和复杂的放射学表现中。
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来源期刊
CiteScore
2.10
自引率
0.00%
发文量
198
审稿时长
1 months
期刊介绍: International Journal of Surgical Pathology (IJSP) is a peer-reviewed journal published eight times a year, which offers original research and observations covering all major organ systems, timely reviews of new techniques and procedures, discussions of controversies in surgical pathology, case reports, and images in pathology. This journal is a member of the Committee on Publication Ethics (COPE).
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